Epinephrine

Product NDC
70518-3173
11-digit product format
705183173
Labeler code
70518
Product ID
70518-3173_c81d65bb-1110-6e82-e053-2995a90a2e29
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Epinephrine
Dosage form
INJECTION
Route
INTRAMUSCULAR; SUBCUTANEOUS
Labeler
REMEDYREPACK INC.
Application
ANDA090589
Marketing category
ANDA
Marketing start
2021-07-27
Marketing end
0000-00-00
Substance
EPINEPHRINE
Active strength
0 mg/.3mL
Pharmacologic classes
Adrenergic alpha-Agonists [MoA],Adrenergic beta-Agonists [MoA],alpha-Adrenergic Agonist [EPC],beta-Adrenergic Agonist [EPC],Catecholamine [EPC],Catecholamines [CS]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70518-3173-02023-03-20C16284748780-1f386c64a-418f-0266-e053-dadaa90a7c1a59dc8445-6cec-40f0-8bde-c23510293509
70518-3173-02023-01-30C16284748780-1f386c64a-418f-0266-e053-dadaa90a7c1a59dc8445-6cec-40f0-8bde-c23510293509

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-3173EPINEPHRINE INJECTION [REMEDYREPACK INC.]5Legacy NDC20241208_59dc8445-6cec-40f0-8bde-c23510293509.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70518-3173-0705183173002 CONTAINER in 1 CARTON (70518-3173-0) > 1 SYRINGE in 1 CONTAINER > .3 mL in 1 SYRINGE2 container2021-07-270000-00-00NoNoCurrent